Ullah Irfan, Escudie Fanny, Scandale Ivan, Gilani Zoela, Gendron-Lepage Gabrielle, Gaudette Fleur, Mowbray Charles, Fraisse Laurent, Bazin Renée, Finzi Andrés, Mothes Walther, Kumar Priti, Chatelain Eric, Uchil Pradeep D
Department of Internal Medicine, Section of Infectious Diseases, Yale University School of Medicine, New Haven, CT 06520, USA.
Drugs for Neglected Diseases Initiative, Geneva, Switzerland.
iScience. 2024 Jan 30;27(3):109049. doi: 10.1016/j.isci.2024.109049. eCollection 2024 Mar 15.
Direct acting antivirals (DAAs) represent critical tools for combating severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants of concern (VOCs) that have escaped vaccine-elicited spike-based immunity and future coronaviruses with pandemic potential. Here, we used bioluminescence imaging to evaluate therapeutic efficacy of DAAs that target SARS-CoV-2 RNA-dependent RNA polymerase (favipiravir, molnupiravir) or main protease (nirmatrelvir) against Delta or Omicron VOCs in K18-hACE2 mice. Nirmatrelvir displayed the best efficacy followed by molnupiravir and favipiravir in suppressing viral loads in the lung. Unlike neutralizing antibody treatment, DAA monotherapy regimens did not eradicate SARS-CoV-2 in mice, but combining molnupiravir with nirmatrelvir exhibited superior additive efficacy and led to virus clearance. Furthermore, combining molnupiravir with caspase-1/4 inhibitor mitigated inflammation and lung pathology whereas combining molnupiravir with COVID-19 convalescent plasma demonstrated synergy, rapid virus clearance, and 100% survival. Thus, our study provides insights into treatment efficacies of DAAs and other effective combinations to bolster COVID-19 therapeutic arsenal.
直接作用抗病毒药物(DAAs)是对抗严重急性呼吸综合征冠状病毒2(SARS-CoV-2)关注变异株(VOCs)的关键工具,这些变异株已逃避基于疫苗诱导的刺突蛋白免疫,以及对抗未来具有大流行潜力的冠状病毒。在此,我们使用生物发光成像技术评估了靶向SARS-CoV-2 RNA依赖性RNA聚合酶(法匹拉韦、莫努匹拉韦)或主要蛋白酶(奈玛特韦)的DAAs对K18-hACE2小鼠体内Delta或Omicron变异株的治疗效果。奈玛特韦在抑制肺部病毒载量方面显示出最佳疗效,其次是莫努匹拉韦和法匹拉韦。与中和抗体治疗不同,DAA单药治疗方案未能在小鼠体内根除SARS-CoV-2,但莫努匹拉韦与奈玛特韦联合使用表现出卓越的相加疗效,并导致病毒清除。此外,莫努匹拉韦与半胱天冬酶-1/4抑制剂联合使用可减轻炎症和肺部病理变化,而莫努匹拉韦与COVID-19康复期血浆联合使用则表现出协同作用、快速病毒清除和100%的存活率。因此,我们的研究为DAAs及其他有效联合用药的治疗效果提供了见解,以增强COVID-19治疗手段。